Quality Investigator — Contract to Full‑Time Opportunity

Kelly Science, Engineering, Technology & Telecom

Raleigh (NC)

Sur place

USD 75 000 - 110 000

Plein temps

Il y a 12 heures
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Résumé du poste

Kelly Science, Engineering, Technology & Telecom is seeking a Quality Investigator to join a regulated manufacturing QA team. You will investigate quality events, perform root cause analyses, support CAPA, and contribute to continuous improvement in a GMP environment.

This is an office-based contract role requiring 3–5 years in FDA-regulated manufacturing, SAP proficiency, and strong documentation and communication skills. Potential to convert to full-time based on business needs.

Qualifications

  • Bachelor's degree in a scientific discipline preferred or relevant experience.
  • 3–5 years of FDA-regulated manufacturing investigation experience.
  • Experience with GMP regulations and quality systems.
  • Proficiency in SAP and MS Office with strong documentation.
  • Excellent written and verbal communication and attention to detail.

Responsabilités

  • Investigate quality events, deviations, and exceptions with root cause analysis.
  • Develop CAPA recommendations and track closure.
  • Support Phase II OOS investigations and audits.
  • Analyze quality metrics and generate KPI reports.
  • Maintain SOPs and quality documentation; participate in continuous improvement.
  • Communicate status updates to leadership and cross-functional teams.

Connaissances

Root cause analysis
CAPA development
Quality documentation
Data analysis
Communication skills
GMP knowledge
PPE wear

Formation

Bachelor's degree in Chemistry, Biology, Microbiology, Engineering

Outils

SAP
Microsoft Office

Description du poste

Kelly Science, Engineering, Technology & Telecom is seeking a Quality Investigator to join a regulated manufacturing QA team. You will investigate quality events, perform root cause analyses, support CAPA, and contribute to continuous improvement in a GMP environment.

This is an office-based contract role requiring 3–5 years in FDA-regulated manufacturing, SAP proficiency, and strong documentation and communication skills. Potential to convert to full-time based on business needs.

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